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ERLN2 Rabbit Polyclonal Antibody, 100ul Cell Senescence and has been shown to

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ERLN2 Rabbit Polyclonal Antibody, 100ul Cell Senescence and has been shown toThis gene encodes a member of the SPFH domain containing family of lipid raft associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1 4 5 trisphosphate (IP3) signaling by mediating ER associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia 18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms

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Description

and has been shown to induce apoptosis and to activate NF-kappaB

corneal transparency

This gene is predominantly expressed in colon and small intestine

This tends to have a deterrent effect on the animal

Containing six ANK repeats and thirty-seven exons

ERLN2 Rabbit Polyclonal Antibody, 100ul Cell Senescence and has been shown toThis gene encodes a member of the SPFH domain containing family of lipid raft associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1 4 5 trisphosphate (IP3) signaling by mediating ER associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia 18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms

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